Creutz C E, Snyder S L, Daigle S N, Redick J
Department of Pharmacology, University of Virginia, Charlottesville 22908, USA.
J Cell Biol. 1996 Mar;132(6):1079-92. doi: 10.1083/jcb.132.6.1079.
Cultures of the nematode C. elegans were examined for the presence of calcium-dependent, phospholipid-binding proteins of the annexin class. A single protein of apparent mass on SDS-polyacrylamide gels of 32 kD was isolated from soluble extracts of nematode cultures on the basis of its ability to bind to phospholipids in a calcium-dependent manner. After verification of the protein as an annexin by peptide sequencing, an antiserum to the protein was prepared and used to isolate a corresponding cDNA from an expression library in phage lambda gt11. The encoded protein, herein referred to as the nex-1 annexin, has a mass of 35 kD and is 36-42% identical in sequence to 10 known mammalian annexins. Several unique modifications were found in the portions of the sequence corresponding to calcium-binding sites. Possible phosphorylation sites in the NH2-terminal domain of the nematode annexin correspond to those of mammalian annexins. The gene for this annexin (nex-1) was physically mapped to chromosome III in the vicinity of the dpy-17 genetic marker. Two other annexin genes (nex-2 and nex-3) were also identified in chromosome III sequences reported by the nematode genomic sequencing project (Sulston, J., Z. Du, K. Thomas, R. Wilson, L. Hillier, R. Staden, N. Halloran, P. Green, J. Thierry-Mieg, L. Qiu, et al. 1992. Nature (Lond.). 356:37-41). The nex-1 annexin was localized in the nematode by immunofluorescence and by electron microscopy using immunogold labeling. The protein is associated with membrane systems of the secretory gland cells of the pharynx, with sites of cuticle formation in the grinder in the pharynx, with yolk granules in oocytes, with the uterine wall and vulva, and with membrane systems in the spermathecal valve. The presence of the annexin in association with the membranes of the spermathecal valve suggests a novel function of the protein in the folding and unfolding of these membranes as eggs pass through the valve. The localizations also indicate roles for the annexin corresponding to those proposed in mammalian systems in membrane trafficking, collagen deposition, and extracellular matrix formation.
对线虫秀丽隐杆线虫的培养物进行检测,以确定是否存在膜联蛋白家族中依赖钙的磷脂结合蛋白。基于其以钙依赖方式结合磷脂的能力,从线虫培养物的可溶性提取物中分离出一种在SDS-聚丙烯酰胺凝胶上表观分子量为32 kD的单一蛋白质。通过肽测序验证该蛋白质为膜联蛋白后,制备了针对该蛋白质的抗血清,并用于从噬菌体λgt11中的表达文库中分离相应的cDNA。编码的蛋白质,在此称为nex-1膜联蛋白,分子量为35 kD,与10种已知的哺乳动物膜联蛋白的序列有36%-42%的同源性。在对应于钙结合位点的序列部分发现了几个独特的修饰。线虫膜联蛋白NH2末端结构域中可能的磷酸化位点与哺乳动物膜联蛋白的位点相对应。该膜联蛋白(nex-1)的基因在物理上定位于III号染色体上dpy-17遗传标记附近。在由线虫基因组测序项目报道的III号染色体序列中还鉴定出另外两个膜联蛋白基因(nex-2和nex-3)(Sulston, J., Z. Du, K. Thomas, R. Wilson, L. Hillier, R. Staden, N. Halloran, P. Green, J. Thierry-Mieg, L. Qiu, et al. 1992. Nature (Lond.). 356:37-41)。通过免疫荧光和使用免疫金标记的电子显微镜技术,将nex-1膜联蛋白定位在线虫中。该蛋白质与咽部分泌腺细胞的膜系统、咽部研磨器中角质层形成部位、卵母细胞中的卵黄颗粒、子宫壁和阴门以及受精囊瓣膜中的膜系统相关。受精囊瓣膜膜与膜联蛋白的结合表明,当卵通过瓣膜时,该蛋白质在这些膜的折叠和展开中具有新功能。这些定位还表明膜联蛋白在膜运输、胶原蛋白沉积和细胞外基质形成中发挥着与哺乳动物系统中所提出的作用相对应的作用。